Our long term goal of this study is to elucidate the roles of annexins II, V and VI and the interactions between annexin V and types II and X collagen in terminal differentiation events of chondrocytes. Terminal differentiation of growth plate chondrocytes consists of a series of events including mineralization and programmed cell death (apoptosis). These events play a crucial role during normal bone formation. If they, however, occur during pathological conditions, such as osteoarthritis, they will lead to cartilage destruction. Thus, an understanding of the cellular mechanisms controlling terminal differentiation of chondrocytes is of great importance. Major advances during the last funding period led to the following three new hypotheses which will be tested in the current proposal: (i) annexin channel formation in the plasma membrane of growth plate chondrocytes and annexin V channel activation by types II and X :ollagen lead to calcium influx into growth plate chondrocytes and alteration of calcium homeostasis; (ii) optimal annexin channel formation and annexin V/collagen interactions require the interactions between annexin II, V and VI; (iii) annexin-mediated alteration of calcium homeostasis regulates terminal differentiation events of growth plate chondrocytes. These hypotheses will be addressed through the following specific aims: 1. We will determine the function of annexin II, V and VI channel formation and annexin V/collagen interactions in alteration of calcium homeostasis in growth plate chondrocytes and test whether annexins through binding to collagen and cytoskeleton act as mechanosensors in these cells. 2. We will determine the interactions between annexin II, V and VI as a possible major regulator of annexin channel formation and annexin V/collagen interactions. 3. We will determine the regulatory roles of annexins and annexin V/collagen interactions in terminal differentiation events including mineralization and apoptosis of growth plate chondrocytes.This study relates directly to the mechanisms which control terminal differentiation of chondrocytes and investigates a novel mechanism regulating calcium homeostasis in skeletal cells.Thus, this proposal will not only greatly advance our understanding of how terminal differentiation events are regulated, but it might also provide novel therapeutic targets to prevent terminal differentiation events during patholoaical conditions.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Research Project (R01)
Project #
5R01AR049074-05
Application #
7235975
Study Section
Orthopedics and Musculoskeletal Study Section (ORTH)
Program Officer
Tyree, Bernadette
Project Start
2003-07-01
Project End
2008-03-31
Budget Start
2007-07-01
Budget End
2008-03-31
Support Year
5
Fiscal Year
2007
Total Cost
$54,467
Indirect Cost
Name
University of Maryland Baltimore
Department
Orthopedics
Type
Schools of Medicine
DUNS #
188435911
City
Baltimore
State
MD
Country
United States
Zip Code
21201
Kirsch, Thorsten (2012) Biomineralization--an active or passive process? Connect Tissue Res 53:438-45
Minashima, Takeshi; Small, William; Moss, Stephen E et al. (2012) Intracellular modulation of signaling pathways by annexin A6 regulates terminal differentiation of chondrocytes. J Biol Chem 287:14803-15
Kim, Hyon Jong; Delaney, John D; Kirsch, Thorsten (2010) The role of pyrophosphate/phosphate homeostasis in terminal differentiation and apoptosis of growth plate chondrocytes. Bone 47:657-65
Kim, Hyon Jong; Minashima, Takeshi; McCarthy, Edward F et al. (2010) Progressive ankylosis protein (ANK) in osteoblasts and osteoclasts controls bone formation and bone remodeling. J Bone Miner Res 25:1771-83
Kirsch, Thorsten; Kim, Hyon Jong; Winkles, Jeffrey A (2009) Progressive ankylosis gene (ank) regulates osteoblast differentiation. Cells Tissues Organs 189:158-62
Kim, Hyon Jong; Kirsch, Thorsten (2008) Collagen/annexin V interactions regulate chondrocyte mineralization. J Biol Chem 283:10310-7
Kirsch, Thorsten (2008) Determinants of pathologic mineralization. Crit Rev Eukaryot Gene Expr 18:1-9
Wang, Wei; Kirsch, Thorsten (2006) Annexin V/beta5 integrin interactions regulate apoptosis of growth plate chondrocytes. J Biol Chem 281:30848-56
Wang, Wei; Xu, Jinping; Kirsch, Thorsten (2005) Annexin V and terminal differentiation of growth plate chondrocytes. Exp Cell Res 305:156-65
Kirsch, Thorsten (2005) Annexins - their role in cartilage mineralization. Front Biosci 10:576-81